SENIOR ENGINEERING TECHNICIAN (SEGUNDO TURNO)

At Johnson & Johnson, the largest healthcare company in the world, we come together for one purpose.
to transform the history of health in humanity.
Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years.
Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest healthcare company in the world.
When You Join Johnson & Johnson, Your Move Could Mean Our Next Breakthrough.
At Johnson & Johnson Medical Devices Companies, we are using our breadth, scale, and experience to reimagine the way healthcare is delivered and to help people live longer, healthier lives.
In a radically changing environment, we are making connections across science and technology to combine our own expertise in surgery, orthopedics, and interventional solutions with the big ideas of others to design and deliver doctor and patient-centric products and solutions.
We are in this for life.
We are changing the trajectory of human health, YOU CAN TOO.
Please visit https://www.
njmedicaldevices.
om/es-419 for more information.
Biosense Webster, Inc.
is recognized worldwide as a leader in the science behind the diagnosis and treatment of cardiac arrhythmias.
Guided by the needs of electrophysiologists and cardiologists, Biosense Webster has pioneered innovative technological advancements for more than 30 years.
Some might call this quite a heritage.
At Biosense Webster, we say it's just the beginning.
For more information, visit www.
iosensewebster.
om DUTIES & RESPONSIBILITIES Under supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position.
Provides support to Principal Technicians or Engineers in matters related to the discipline.
Follows standardized procedures to perform his/her tasks, when applicable.
Maintains his/her work area clean and organized.
Initiates, adjusts, and operates basic laboratory and manufacturing equipment.
Has completed the environmental and safety training, appropriate for his/her discipline.
Writes technical reports in a moderate complexity manner, using graphics, and schemes to describe and illustrate operative characteristics of the system/tests, as well as dysfunctions, deviations about the specifications of designs and functional limitations.
Solves problems related to the systems, components and electrical equipment, testing, mechanical, hydraulics or of installation.
Performs basic operational diagnostics tests, solves problems and disconnects components, subassemblies and manufacturing systems, processes and equipment with the purpose of isolating the failures, determine a solution and perform the necessary operations.
Documents all the changes.
Ensures that the tools and testing equipment are properly calibrated and repaired, according to the standardized operations procedures.
Provides support and/or performs equipment and fixtures quotation processes for preparation for the purchasing process.
Provides support in the installation and validation processes of equipment required in the assigned area.
Provides support in the SPC process statistical control processes where applicable.
Provides support and/or generates Engineering changes or ECOs.
Correctly develops the equipment and fixture’s introduction process to clean room following procedures and requirements established, such as, for example, MAL, PM and calibrations to it.
Enters his/her daily tasks in eCMMS or in the system assigned for that purpose.
Responsible for communicating business related issues or opportunities to next management level.
Responsible for ensuring subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition.
Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
Performs other duties assigned as needed.
Qualifications EXPERIENCE AND EDUCATION Knowledge and skills to satisfactorily develop the responsibilities of the position.
6 to 8 years of experience preferably related to the position.
High School, technical career or equivalent.
Preferably trained in two or more of the following disciplines.
electronics, mechanics, production, electro-mechanics, testing, quality and production and process statistical control, bio-medics or industrial.
Desirable experience (current or previous) in the medical products industry.
Desirable 60% English REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS Basic ability to read and understand technical documentation associated to the specific discipline.
GMPs (Good Manufacturing Practices) / ISO knowledge, preferably.
Knowledge of preventive and corrective maintenance, documentation, calibration procedures and quality systems, preferably.
Ability to use computers and related software.
Ability to use measuring and testing equipment associated with the specific discipline.
Knowledge of the Campus information systems, preferably.
Ability to successfully complete the departmental / corporate training courses in manufacturing techniques.
Ability to use the internal documentation change system (CPDM).